Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g24140 | A01 | 12637853 | C | T | missense_variant | MODERATE | c.934G>A|p.Asp312Asn |
S78 |
2 | BAA01g24140 | A01 | 12637954 | G | A | missense_variant | MODERATE | c.833C>T|p.Thr278Ile |
S197 |
3 | BAA01g24140 | A01 | 12638245 | C | T | missense_variant | MODERATE | c.751G>A|p.Val251Ile |
S256 |
4 | BAA01g24140 | A01 | 12638279 | C | T | synonymous_variant | LOW | c.717G>A|p.Lys239Lys |
S202 |
5 | BAA01g24140 | A01 | 12638692 | G | A | missense_variant | MODERATE | c.560C>T|p.Ser187Phe |
S234 |
6 | BAA01g24140 | A01 | 12639651 | C | T | missense_variant | MODERATE | c.67G>A|p.Glu23Lys |
S280 |
7 | BAA01g24140 | A01 | 12639659 | G | A | missense_variant | MODERATE | c.59C>T|p.Thr20Ile |
S293 |
8 | BAA01g24140 | A01 | 12643367 | G | A | upstream_gene_variant | MODIFIER | c.-3650C>T| |
S190 |
9 | BAA01g24140 | A01 | 12643883 | G | A | upstream_gene_variant | MODIFIER | c.-4166C>T| |
S40 S49 |
10 | BAA01g24140 | A01 | 12643982 | G | A | upstream_gene_variant | MODIFIER | c.-4265C>T| |
S36 |